## Dedicated to Professor Wei-Yuan Huang on the occasion of his 85th birthday The 1,3-dipolar cycloaddition of azomethine ylides to electron-deficient alkenes is one of the most powerful methods for the construction of highly substituted pyrrolidine rings. [1] Following early research on the prepa
A Highly Enantio- and Diastereoselective Cu-Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with Nitroalkenes.
β Scribed by Xiao-Xia Yan; Qian Peng; Yan Zhang; Kai Zhang; Wei Hong; Xue-Long Hou; Yun-Dong Wu
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 40 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
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on the occasion of his 85th birthday The 1,3-dipolar cycloaddition of azomethine ylides to electron-deficient alkenes is one of the most powerful methods for the construction of highly substituted pyrrolidine rings. [1] Following early research on the preparation of optically active pyrrolidines in
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v